- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT07681596
A Modular, Phase I/II, Multicentre Study to Evaluate AZD4045, in Participants With Relapsed or Refractory Multiple Myeloma
A Modular, Phase I/II, Open-label, Multicentre Study to Evaluate the Safety, Tolerability, Cellular Kinetics, and Efficacy of AZD4045, an Allogeneic Chimeric Antigen Receptor-T Cell (CAR-T) Therapy Targeting B Cell Maturation Antigen (BCMA) in Participants With Relapsed or Refractory Multiple Myeloma
연구 개요
상세 설명
연구 유형
등록 (추정된)
단계
- 2 단계
- 1단계
연락처 및 위치
연구 연락처
- 이름: AstraZeneca Clinical Study Information Center
- 전화번호: 1-877-240-9479
- 이메일: information.center@astrazeneca.com
연구 장소
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California
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Duarte, California, 미국, 91010
- 모병
- Research Site
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Colorado
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Denver, Colorado, 미국, 80218
- 아직 모집하지 않음
- Research Site
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Florida
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Tampa, Florida, 미국, 33612
- 아직 모집하지 않음
- Research Site
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Georgia
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Atlanta, Georgia, 미국, 30322
- 아직 모집하지 않음
- Research Site
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Missouri
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St Louis, Missouri, 미국, 63110
- 아직 모집하지 않음
- Research Site
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New Jersey
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Hackensack, New Jersey, 미국, 07601
- 아직 모집하지 않음
- Research Site
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Ohio
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Cleveland, Ohio, 미국, 44195
- 아직 모집하지 않음
- Research Site
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Tennessee
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Nashville, Tennessee, 미국, 37203
- 아직 모집하지 않음
- Research Site
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Texas
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Houston, Texas, 미국, 77030
- 아직 모집하지 않음
- Research Site
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Wisconsin
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Milwaukee, Wisconsin, 미국, 53226
- 아직 모집하지 않음
- Research Site
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Camperdown, 호주, 2050
- 아직 모집하지 않음
- Research Site
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East Melbourne, 호주, 3002
- 모병
- Research Site
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참여기준
자격 기준
공부할 수 있는 나이
- 성인
- 고령자
건강한 자원 봉사자를 받아들입니다
설명
Inclusion Criteria:
- Participant must be 18 years or older at the time of signing the informed consent form.
- Participants must have documented diagnosis of MM according to the IMWG diagnostic criteria.
Participant must have one or more of the following measurable disease criteria:
- Serum M-protein level ≥ 1.0 g/dL.
- Urine M-protein ≥ 200 mg/24 h.
- Serum immunoglobulin free light chain ≥ 10 mg/dL (100 mg/L) and abnormal serum immunoglobulin kappa lambda free light chain ratio.
- ECOG performance score of 0 to 1.
- Participant must have screening bone marrow aspirate and/or archival sample adequate for clonal sequence calibration for MRD. An archival sample obtained from any time prior is acceptable.
- Participant must have adequate organ and bone marrow function.
- Participant must have received at least 3 prior classes of therapy, including a PI, an IMiD, and an anti-CD38 antibody
- Participant must have documented evidence of PD by IMWG 2016 criteria based on Investigator's determination during or after the most recent line of therapy
Exclusion Criteria:
- Participant has a history of any grade IEC-HS and/or history of Grade ≥ 3 CRS and/or Grade ≥ 2 neurotoxicities during prior CAR-T cell therapy or T cell engaging therapy.
- Participant has ongoing toxicity from previous anti-cancer therapy that did not resolve to baseline levels or to Grade ≤ 1 with the exception of alopecia or peripheral neuropathy.
- Participant has a known active, or prior history of CNS involvement or exhibits clinical signs of meningeal involvement of MM.
- Participant has systemic immunoglobulin light chain amyloidosis, active plasma cell leukaemia (presence of ≥ 5% of circulating plasma cells on a conventional peripheral blood smear) at time of screening, Waldenstrom macroglobulinemia or Polyneuropathy Organomegaly Endocrinopathy M-protein and Skin (POEMS) syndrome.
- Participant has a history of haematologic malignancies, other than MM, regardless of remission status.
- Participant has a history of a prior non-haematologic malignancy unless the participant has been disease-free with no evidence of recurrence for ≥ 2 years.
- Participant has significant neurological or psychiatric condition (active or history of).
Participant is positive for any of the following:
- HIV (with exceptions)
- Chronic or active hepatitis B
- Active hepatitis C
Participant has clinically significant cardiovascular disease, including but not limited to:
- Myocardial infarction within 6 months prior to eligibility confirmation, or an unstable or uncontrolled disease/condition related to or affecting cardiac function.
- Uncontrolled cardiac arrhythmia or clinically significant ECG abnormalities.
- Congestive heart failure Class III or IV.
- Impaired cardiac function (LVEF < 45%).
Participant has any other significant medical condition which, in the opinion of the Investigator, places the participant at an unacceptable risk for treatment-related complications, could interfere with the successful or safe delivery of therapy, or could interfere with evaluation of study intervention or interpretation of participant safety or study results. These include but are not limited to:
- Serious active or uncontrolled infection.
- Requirement of supplemental oxygen to maintain oxygen saturation.
- Active autoimmune disease or a history of autoimmune disease within 2 years.
- Inflammatory bowel disease requiring treatment within the past 5 years or other clinically significant gastrointestinal condition.
- Participant received live, attenuated vaccine within 28 days prior to eligibility confirmation
- Participant has undergone major surgery within 28 days prior to eligibility confirmation
- Concurrent enrolment in another clinical study (unless the study is observational, or the participant is in the follow-up period of an interventional study).
- Participant has a known life-threatening allergy, hypersensitivity, intolerance, or a contraindication to any study intervention or their excipients.
- Participant received any prior CAR-T or CAR-NK therapy directed at any target within 6 months prior to eligibility confirmation.
- Participant received any prior TCE therapy directed at any target within 6 months prior to eligibility confirmation.
- Participant received any prior BCMA-targeted treatment within 6 months prior to eligibility confirmation.
- Participant with a history of refractoriness to the most recent BCMA-targeted treatment received as defined as PD on or within 60 days of last dose or non-responsiveness (ie, did not achieve at least minimal response) on therapy.
- Participant received prior allogeneic stem cell transplant at any time.
- Participant received autologous stem cell transplant within 3 months prior to eligibility confirmation.
- Participant received radiation therapy for treatment of plasmacytoma within 14 days before eligibility confirmation.
Participant received prior anti-tumour therapy as follows prior to the first dose of lymphodepletion:
a) Within 7 days:
- Immunomodulatory or cereblon E3 ligase modulatory drugs. b) Within 14 days:
- PI therapy.
- Monoclonal antibody treatment for MM.
- Cytotoxic therapy.
- Other systemic anti-myeloma therapy.
- Radiation. c) Within 14 days or at least 5 half-lives, whichever is longer:
- Targeted therapy, epigenetic therapy, investigational drug or used an invasive investigational medical device.
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 무작위화되지 않음
- 중재 모델: 병렬 할당
- 마스킹: 없음(오픈 라벨)
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
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실험적: Module 1: AZD4045 monotherapy
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Allogeneic Chimeric Antigen Receptor T cell (CAR-T) Therapy Targeting B Cell Maturation Antigen (BCMA)
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실험적: Module 1: AZD4045 in association with daratumumab and aldesleukin
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Allogeneic Chimeric Antigen Receptor T cell (CAR-T) Therapy Targeting B Cell Maturation Antigen (BCMA)
Anti-CD38 monoclonal antibody
Recombinant human IL-2
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연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
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Adverse events (AEs) and serious AEs (SAEs)
기간: Through study completion, an average of 2 years
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Incidence and severity of adverse events (AEs) and serious AEs (SAEs)
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Through study completion, an average of 2 years
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Dose-limiting toxicities (DLT)
기간: 28 days
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Incidence and severity of dose-limiting toxicity (DLT) events
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28 days
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2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
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Efficacy - Objective Response Rate (ORR)
기간: Through study completion, an average of 2 years
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Defined as proportion of participants who achieve an overall response of PR or better according to the IMWG 2016 criteria
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Through study completion, an average of 2 years
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Efficacy - Complete Response Rate (CRR)
기간: Through study completion, an average of 2 years
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Defined as proportion of participants who achieve a CR/sCR response according to the to the IMWG 2016 criteria
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Through study completion, an average of 2 years
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Efficacy - Duration of Response (DOR)
기간: Through study completion, an average of 2 years
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Defined as the time from first documented confirmed response until date of documented PD per IMWG 2016 criteria or death due to any cause, whichever occurs first
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Through study completion, an average of 2 years
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Efficacy - Time to Response (TTR)
기간: Through study completion, an average of 2 years
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Defined as the time from infusion until the date of first documented objective response, as assessed per IMWG 2016 criteria
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Through study completion, an average of 2 years
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Cellular kinetics - Quantification of CAR transgene levels
기간: Through study completion, an average of 2 years
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Determination of transgene level
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Through study completion, an average of 2 years
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Cellular kinetics - Tmax
기간: Through study completion, an average of 2 years
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Time to reach maximum AZD4045 level
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Through study completion, an average of 2 years
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Cellular kinetics - Cmax
기간: Through study completion, an average of 2 years
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Maximum AZD4045 level
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Through study completion, an average of 2 years
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Cellular kinetics - AUC0-28d
기간: 0 - 28 days
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Area under the concentration time-curve of AZD4045 level
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0 - 28 days
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Cellular kinetics - Tlast
기간: Through study completion, an average of 2 years
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Time to last quantifiable concentration of AZD4045 level
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Through study completion, an average of 2 years
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Cellular kinetics - Clast
기간: Through study completion, an average of 2 years
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Observed concentration of AZD4045 at last quantifiable concentration
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Through study completion, an average of 2 years
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Cellular kinetics - AUClast
기간: Through study completion, an average of 2 years
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Area under the concentration time-curve of AZD4045 level
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Through study completion, an average of 2 years
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공동 작업자 및 조사자
스폰서
연구 기록 날짜
연구 주요 날짜
연구 시작 (실제)
기본 완료 (추정된)
연구 완료 (추정된)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
추가 관련 MeSH 약관
기타 연구 ID 번호
- D7540C00001
개별 참가자 데이터(IPD) 계획
개별 참가자 데이터(IPD)를 공유할 계획입니까?
IPD 계획 설명
Qualified researchers can request access to anonymized individual patient-level data from AstraZeneca group of companies sponsored clinical trials via the request portal Vivli.org. All requests will be evaluated as per the AZ disclosure commitment:
https://astrazenecagrouptrials.pharmacm.com/ST/Submission/Disclosure.
Yes, indicates that AZ are accepting requests for IPD, but this does not mean all requests will be shared.
IPD 공유 기간
IPD 공유 액세스 기준
When a request has been approved AstraZeneca will provide access to the anonymized individual patient-level data via secure research environment Vivli.org.
Signed Data Usage Agreement (non-negotiable contract for data accessors) must be in place before accessing requested information.
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
미국 FDA 규제 기기 제품 연구
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .